Dr. Douglas Gabriel posted this article back in September 2021. We are re-publishing it below at the request of some readers.
Plandemic Criminals – Indictable Evidence
Dr. Richard M. Fleming has given all the indictable evidence we need to start arresting and convicting the criminals behind the current plandemic that has devastated the entire world economically and killed and maimed millions globally. His book: Is COVID-19 a Bioweapon, A Scientific and Forensic Investigation provides the blow-by-blow plan to create a viral bioweapon of mass destruction. He provides the proof of the U. S. sources of funding to the criminals who set out to violate all laws concerning gain-of-function biological research to create a laboratory created synthetic virus that was designed to kill as many people as possible. He offers the original documents that prove Anthony Fauci and his gang of bio-criminals at the National Institutes of Health (NIH), the Center for Disease Control and Prevention (CDC), and many other U. S. Federal agencies used to gain grants and patents to turn public laboratories into killing machines with U. S. taxpayer monies. He also gives the dates and contents of publications wherein these criminals brag about their research to the world without shame and with seeming impunity.
We have summarized and condensed the excellent work of Dr. Fleming into a readable form for layman who might not be familiar with medical terms concerning this deadly research. Fleming does not draw conclusions or demand judicial action to be taken against these “war actors”, but you will yourself, no doubt, come to the same conclusions that we did when presented with the overwhelming evidence that shows the broad trail of crimes that have led to our current world dilemma. You will surely ask the question, Why aren’t these criminals in jail and being held accountable for their consciously perpetrated crimes? This question, which is inevitable, needs to be addressed by law enforcement, the Department of Justice, the U. S. Congress, the president of the United States and any honest judges left in this country to defend U. S. Civil Rights and the United States Constitution. These crimes must be prosecuted if freedom and life as we know it are to continue to go on in America.
In 2002, following the SARS-CoV-1 outbreak in China, Dr. Shi Zhengli-Li and colleagues at the Wuhan Institute of Virology began investigating how SARS-CoV-1 was transmitted. In particular Zhengli was interested how SARS-CoV-1 was transmitted from person to person. To do this, she developed chimeric (Gain-of-Function) coronaviruses using human immunodeficiency, virus-based pseudovirus systems (laboratory man-made viruses) with the cell lines of people, civet cats, and horseshoe bats. In March 2004, the US Health and Human Services agency announced that it was going to create the National Science Advisory Board for Biosecurity to be managed by the National Institutes of Health, thus consciously violating U. S. laws prohibiting such research. In 2005, Dr. Ralph Baric published a paper declaring he could alter the genome of coronaviruses. In 2006, using chimeric (Gain-of-Function) research, Chinese scientists in Wuhan reported their ability to combine parts of four different viruses into a single viral genome. They combined parts of four viruses: hepatitis C, human immunodeficiency virus (HIV-1, AIDS), SARS-CoV-1, and SARS-CoV-2. Thus, COVID-19 was made in a laboratory as an attempt to kill human beings.
When the Swine Flu vaccine of the mid-1970s produced neurological damage, including Guillain-Barre syndrome, following the first twenty-five deaths, the swine flu vaccine and vaccination program was stopped by the U. S. government. Today the Vaccine Adverse Event Reporting System (VAERS) shows thousands of deaths following SARS-CoV-2 vaccinations with over 400,000 experiencing severe adverse effects, and yet, this CDC provide data has not ended the use of COVID vaccines (DNA manipulation fake-vaccine) and the harmful vaccination program killing and harming Americans.
Two published papers looking at the consequences of the SARS-CoV-2 spike protein penetrating the brain of humanized mice and rhesus macaques show brain inflammation, mad cow disease (Spongiform encephalopathy), and Alzheimer disease. (Mariano Caroosino et al., January 2021 & Ingrid HCHM Philippens et al., May 5, 2021.) In other words, even though all of the mice showed damaging inflammation in their lungs, all the animals died due to brain damage with the virus entering the brain though the olfactory system (nose).
It is critical to understand that it makes no difference whether the spike protein of SARS-CoV-2 is introduced into the body via person-to-person transfer or via injection of biologicals (vaccines), the effect is the same.
In 2012, an investigation into Gain-of-Function research resulted in a voluntary moratorium that lasted almost one year and ended in January 2013 due to the dangers of biological experimentation concerning all viruses. In 2014, shortly thereafter, Ralph Baric and Chinese researchers published a paper demonstrating the differences between spike proteins that can infect bats and those capable of infecting people. This research was funded by National Institutes of Health grants RO1AI089728 and R21AI109094. In October of 2014, only one year after lifting the moratorium, the Obama Administration placed a ban on Gain-of-Function research after it was discovered that the CDC had accidentally exposed workers to Anthrax and “unwittingly” shipped out samples of influenza virus contaminated with the deadly H5N1 virus.
In 2015, Baric and Zhengli both announced they had “reengineered, through Gain-of-Function, the spike protein of coronavirus so they could infect human cells.” (Y. Yang et al., Journal of Virology 89, no 17, 2015) This research was paid for by NIH grants RO1AI089728 and RO1AI110700. Recommendations for the oversight of Gain-of-Function research were made on April 7, 2016, and approved on March 15, 2016, by the National Science Advisory Board for Biosecurity. Dr. Anthony Fauci is an ex officio member of that board. But this notwithstanding, the research moved forward in America and China.
Laws Concerning Gain-of-Function Research
The U. S. law that will put bioweapon makers and funders into jail is:
United States Federal Code 12 U.S.C. Chapter 10–175 – which expressly prohibits such biological weapons and makes it a criminal offence.
“175. Prohibitions with respect to biological weapons
(a) In General. – Whoever knowingly develops, produces, stockpiles, transfers, acquires, retains, or possesses any biological agent, toxin, or delivery system for use as a weapon, or knowingly assists a foreign state or any organization to do so, or attempts, threatens, or conspires to do the same, shall be fined under this title or imprisoned for life or any term of years, or both.”
Other provisions for prosecution of bioweapon makers, producers, conspirators:
Biological Weapons Convention Treaty of 1969 – signed and ratified by the United States of America in 1972. It is a violation of the treaty to develop, acquire, retain, or produce any biological agent or toxin that has no justification for prevention or peaceful purposes.
The Nuremberg Code 1947 – includes such principles as informed consent, absence of coercion, properly formulated scientific experimentation, and demands beneficence towards experiment participates.
International Covenant on Civil and Political Rights-1976 – provides for respect for civil and political rights of individuals, including the right to life, freedom of religion, freedom of speech, freedom of assembly, electoral rights, and rights to due process.
In October of 2014, the US government issued a policy statement regarding Gain-of-Function research including the following restrictions:
“New [US government] funding will not be released for gain-of-function research projects that may be reasonably anticipated to confer attributes to influenza, MERS, or SARS viruses such that the virus would have enhanced pathogenicity and/or transmissibility in mammals via the respiratory route.”
Cast of Criminals
Dr. Anthony Fauci – NIH, NIAID
Robert Redfield – US Centers for Disease Control and Prevention (Toxic Substances)
Dr. Ralph Baric – Carolina Vaccine Institute at the University of North Carolina
Dr. Shi Zhengli-Li – Wuhan Institute of Virology
Dr. Deborah Birx – CDC, Coronavirus Coordinator, Division of Global HIV/AIDS
Dr. Shibe Jiang – Shanghai Medical School Fudan University
Dr. Fang Li – Beijing University
Peter Daszak – EcoHealth Alliance
Colonel David Franz – Deputy Commander of Fort Detrick, US Biological Weapons Division
Amongst many others…
We can find the criminals behind the plandemic by looking at publications and documents from the Department of Defense, National Institute of Health (National Institute of Allergy and Infectious Diseases), Centers for Disease Control and Prevention, Food and Drug Administration, Health and Human Services, National Science Foundation, EcoHealth Alliance, U. S. Agency for International Development, Department of Commerce, Department of Agriculture, Department of the Interior, U. S. Patent and Trademark Office, National Biosurveillance Integration Center, and other federal agencies.
1974 – The first reported genetically altered (Gain-of-Function) virus QB phage was created.
1985 – Ralph Baric began working with coronaviruses in the mid-1980s. In 1985, while at the University of California (UCLA) conducted research on recombinant viruses, including coronaviruses which was paid for by the National Science Foundation and U. S. Public Health and Human Services agency (HHS) by grant A1 19244.
2000 – Researcher in Spain and Paul Ahlquist from the University of Wisconsin showed how combining complementary DNA with nuclear expression of RNA allowed the researchers to develop a synthetic virus. The spike protein of the virus was replaced with the spike protein from another virus creating a chimeric (Gain-of-Function) virus that infected the gastrointestinal system of pigs. The researchers discovered this could now be done with dogs, cats, and humans.
2000 – With funding from NIH (Grant A1 239476) Ralph Baric and others enhanced a transmissible gastroenteritis virus. This infective transmissible virus, produced synthetically in a laboratory, was indistinguishable from the wild-type virus.
2001 – German researchers used smallpox virus DNA to produce an infectious coronavirus using restriction enzymes that work like molecular scissors to cut DNA and ligate it into a vector. (Masters, 1999; Almazan et al., 2000; Yount et al., 2000). With this DNA manipulation, it became possible to rapidly generate a large collection of genetically modified coronaviruses. Expression of multiple subgenomic mRNAs in infected coronaviruses formed the basis of creating vector systems, each encoded with heterologous protein. These features could then be exploited in the development of a new class of RNA vaccine vectors.
2001 – In May, Ralph Baric and colleagues applied for a patent to manipulate genes and profit from genetic manipulation of plants, animals, bacteria, and viruses – including coronaviruses. The patent was granted on July 15, 2003. This research was supported by U. S. taxpayer monies.
2003 – Baric and others published research funded by NIH (grants A123946, GM63228, A126603) showing they could rescue SARS-CoV Urbani viruses by using reverse genetics. They then could fully clone SARS viruses. This process increased the infectivity for SARS-CoV-2 and has been shown to insert its genetic sequence into the human DNA. This research was funded by the NIH (1U19AI131135-01, 5R01MH104610-21).
2006 – Chinese researchers spliced four target cDNA segments together to form a single 1,200-nucleotide-long RNA sequence. This chimeric (Gain-of-Function) sequence included combining hepatitis C viruses, human immunodeficiency virus (HIV-1 AIDS), and SARS-CoV-2.
2007 – In May, a patent was granted for isolation of human SARS-Co-V-1 to the U. S. Department of Health and Human Services agency (HHS). This established the polymerase chain reaction (PCR) test to find the virus. In April, 2020, the FDA issued an umbrella Emergency Use Authorization for PCR testing of SARS-Co-V-2.
2007 – Dr. Zhengli and colleagues in Australia demonstrated that insertions placed in spike proteins made it possible for SARS-CoV to infect human cells.
2013 – Baric and colleagues discovered four critical genes that were expressed following SARS-CoV infections that created lung damage through fibrin that caused blood clotting. This was funded by NIAID, NIH, HHS, and the National Center for Advancing Translational Sciences (HHSN272200800060C; 5UL1RR02414).
2014 – In March, Baric applied for an international patent for the Methods and Compositions for Chimeric (Gain-of-Function) Coronavirus Spike Proteins with support from NIH grant U54AI057157.
2014 – Dr. Li Meng Yan discovers that SARS-CoV-1 was a genetically modified (Gain-of-Function) virus that was a bioweapon developed by the Chinese Communist Party, with SARS-CoV-2 being the upgraded version of this bioweapon.
2015 – Baric and Zhengli received funding from Peter Daszak of EcoHealth Alliance and NIH to publish their research that had used reverse genetics to generate a pathogenic chimeric virus, formed from parts of various animals, that could not be controlled by the use of drugs and could cross the blood-brain barrier of humans. They concluded that these viruses were able “to replicate in human airway cultures, cause pathogenesis, and escape current therapeutics.” Further funding for this bioweapon came from National Natural Science Foundation of China, the Wuhan Institute of Virology, University of North Carolina, University of Texas Medical Branch, USAID, and the U. S. Central Intelligence Agency (CIA).
2015 – In September, Zhengli and Baric reengineered, through mutations (Gain-of-Function), the spike protein of MERS to increase infectivity of humans through viral entry into human cells. (NIH Grants RO1AI089728, RO1AI110700).
2015 – Peter Daszak and EcoHealth Alliance denounce a laboratory origin of this virus insisting on a zoonotic (animal) origin of this bioweapon.
2012 – In January, Peter Daszak leads the World Health Organization “team of experts” to the Wuhan Institute of Virology and insists the great amount of missing documents concerning SARS-CoV-2 was irrelevant. No connection between SARS-CoV-2 and the Wuhan laboratory was found by Daszak’s team.
This timeline of crime is proof positive of the crimes against humanity that the Cast of Criminals and their agents have committed by creating a biological Weapon of Mass Destruction. The time has come for them to answer for their crimes.
Big-Pharma’s Pharmaceutical WWIII started with numerous actions Donald Trump took, while president, that demonstrated that he is either an idiot, or he was/is/became an agent of Big-Pharma before he signed Executive Order 13887 expanded the definition of viruses and giving a blank check to the WHO/CDC/NIH to experiment on humans with dangerous vaccine-like drugs that are actually bioweapons. It seems like the loss of life, like the 100,000 or so who die from influenza each year in America (65% of whom received the flu vaccine), are statistically incidental in the “research” to find a perfect vaccine for all influenza viruses. This desperate need to “stop the common flu and cold” has, in turn, created a BIOECONOMY that raked in more than five trillion dollars (+) for Covid – which was nothing more than the yearly flu.
The “biotechnology” of vaccines is now the biggest global industry, even above warmongering, and with the endless “booster” shots, will soar to new heights beyond any warmongering snake-oil scam or Ponzi scheme in history. To think, the best killer-fraud of all times was pulled off with the murderers being given prior, and complete, immunity because Trump and Biden’s Executive Orders and actions gave Big-Pharma control of American sovereignty through WHO/CDC/NIH medical tyranny that has overthrown the US Constitution and Bill of Rights. The United Nations has been in control of the world since the fake-pandemic was “pronounced” from the infallible church of holy science’s global offices at of the World Health Organization – Big-Pharma’s agents. These supposed experts killed more people via their protocols, mandates, and bad medical advice than Covid did.
All of these political machinations that have abnegated the US Constitution are supposedly legal due to the Pandemic and All Hazards Preparedness Act of 2019, and the 21st Century Cures Act of 2016, that assign all control of Americans during a pandemic to the World Health Organization via the CDC and NIH. This pandemic fraud surrenders our American sovereignty to an agency of the United Nations under the guise of medical safety and security. These treasonous “laws” gave the legal right for the heinous acts of the six million medical iatrogenic deaths called Covid. This is simply death by doctors and drugs.
CDC Influenza and pneumonia vaccine shot statistics demonstrate that these vaccines simply create more influenza and pneumonia. Vaccines have never worked, and the CDC now admits that they added viruses as pathogens to childhood vaccines in the past that eventually caused over 100 million cancer cases. And yet, we haven’t taken our pitchforks and surrounded the WHO/CDC/NIH and stopped their obvious planned eugenics. Depopulation is the number one issue for the United Nations. Their agencies work for the demise of millions through vaccines that sterilize, polio shots that create polio, peace-keepers who rape and kill, economic agencies (World Bank, WTO, IMF, etc.) who steal and fleece undeveloped nations and manipulate the rest, and the many other atrocities they are well-known for. When Trump defunded the United Nations by 50%, many thought there was hope. But, when Trump either fell for, or aligned with the fake pandemic plan, he turned to the dark side and hasn’t come back yet. This is also evidenced in his lightning-fast response to the outbreak by calling a National Health Emergency (Jan 27), closing air travel from China (Jan 31), proclaiming a National Emergency on March 1 (ratified on March 13), agreeing to the WHO declaration of a Global Pandemic on March 11, creating Emergency Use Authorization for fake vaccines on January 13, allowing Ivermectin to be outlawed by the FDA on April 10, and fathering Operation Warp Speed on April 29.
Understanding this timetable demonstrates that Trump was part of the plan to frighten Americans into taking an experimental bioweapon drug [vaccine] for an incidental virus. There was no historical precedent for abnegating all the rules and going headlong into creating a supposedly permanent vaccine for “all” influenza-like viruses. Only after Trump declared a National Health Emergency could the rules and regulations be thrown out. Trump proclaimed the fake-pandemic on January 27, even before the WHO proclaimed a Global Pandemic. Trump was the cheer leader of vaccines even before Covid was “thought of”, as seen by his September 19, 2019 Executive Order. He is still cheer leading as the “King of the Vaccine” that supposedly saved “millions of lives.” If we look at the timetable closely, the circumstantial evidence is quite convincing that Trump and Biden are simply agents of Big-Pharma.
Pharmaceutical WWIII – the Fake Virus X and Permanent Vaccines
Executive Order 13887, September 19, 2019, Donald Trump – Modernizing Influenza Vaccines in the United States toPromote National Security and Public Health
Translation: The sanctioning of experimental vaccines including gain-of-function bioweapons.
President Donald Trump issued Executive Order 13887 on Thursday, September 19, 2019, in an attempt to improve and modernize influenza vaccine manufacturing processes to develop vaccines that provide more effective and longer lasting protection. Under the order, a National Influenza Vaccine Task Force was established. The goal of the Task Force is to compile a report, which includes a 5-year plan to promote new vaccine manufacturing technology and to accelerate the development of a universal flu vaccine.
Translation: Trump sold out to Big-Pharma since corona viruses (Covid) are considered equivalent to influenza. This EO was written before Covid-19 ever came along. Big-Pharma wrote this EO so they could pull-off the pandemic scam. The word pandemic appears repeatedly throughout this EO and basically makes Big-Pharma a government monopoly with full immunity from liability. It sanctions cell manipulation [m-RNA] and new types [viral vectors, pegylated graphene oxide, etc.] of vaccines. Thus, the definition of a vaccine is changed through this EO and allows experimental vaccine research and development.
Sec. 2. This order directs actions to reduce the United States’ reliance on egg-based influenza vaccine production; to expand domestic capacity of alternative methods that allow more agile and rapid responses to emerging influenza [corona] viruses; to advance the development of new, broadly protective vaccine candidates that provide more effective and longer lasting immunities; and to support the promotion of increased influenza vaccine immunization across recommended populations.
Translation: Get ready for Frankenstein vaccines which are supposed to kill “elusive” diseases. You will be coerced into taking toxic vaccines, without informed consent.
(i) a 5-year national plan (Plan) to promote the use of more agile and scalable vaccine manufacturing technologies and to accelerate development of vaccines that protect against many or all influenza viruses;
(ii) recommendations for encouraging non-profit, academic, and private-sector influenza vaccine innovation;
(A) estimate the cost of expanding and diversifying domestic vaccine manufacturing capacity to use innovative, faster, and more scalable technologies, including cell-based [genomic] and recombinant vaccine manufacturing [mRNA], through cost-sharing agreements with the private sector, which shall include an agreed-upon pricing strategy during a pandemic;
(E) evaluate incentives for the development and production of vaccines by private manufacturers and public-private partnerships, including, in emergency situations,the transfer of technology to public-private partnerships – such as the HHS Centers for Innovation and Advanced Development and Manufacturing or other domestic manufacturing facilities – in advance of a pandemic, in order to be able to ensure adequate domestic pandemic manufacturing capacity and capability;
Translation: This EO is predicting the pandemic and making plans to give control to the private sector, supplied with endless government money, to experiment with new drugs without any responsibility or accountability.
(A) further implement vaccine production process improvements to reduce the time required for vaccine production;
(C) further support the conduct, in collaboration with the DOD, BARDA, and CDC, of applied scientific research regarding developing cell lines and expressionsystems that markedly increase the yield of cell-based and recombinant influenza vaccine manufacturing processes; and
(v) through the Administrator of CMS, examine the current legal, regulatory, and policy framework surrounding payment for influenza vaccines and assess adoption of domestically manufactured vaccines that have positive attributes for pandemic response (such as scalability and speed of manufacturing).
Translation: It is OK to use previously failed experimental viral vectors and mRNA vaccines that have been proven harmful and lethal.
Timeline of Lost Battles in the Pharmaceutical WWIII
Let’s examine the dates of each of the first battles in the fake pandemic to demonstrate that Trump and Biden are good-old-boys working for the drug companies and their minions at the WHO/CDC/NIH.
Executive Order 13887, September 19, 2019, Donald Trump – Modernizing Influenza Vaccines in the United States toPromote National Security and Public Health
The Secretary of Health and Human Services (Alex Azar) declared a Public Health Emergency on January 27, 2020, under section 319 of the Public Health Service Act (42 U.S.C. 247d), in response to COVID-19.
Proclamation 9994 of March 13, 2020: Declaring a National Emergency Concerning the Novel Coronavirus Disease (COVID-19) Outbreak:
NOW, THEREFORE, I, DONALD J. TRUMP, President of the United States, by the authority vested in me by the Constitution and the laws of the United States of America, including sections 201 and 301 of the National Emergencies Act (50 U.S.C. 1601 et seq.) and consistent with section 1135 of the Social Security Act (SSA), as amended (42 U.S.C. 1320b-5), do hereby find and proclaim that the COVID-19 outbreak in the United States constitutes a National Emergency, beginning March 1, 2020.”
The World Health Organization (WHO) on March 11, 2020, declared the novel coronavirus (COVID-19) outbreak a Global Pandemic. WHO Director-General, Dr. Tedros Adhanom Ghebreyesus, noted that over the past two weeks, the number of cases outside China increased 13-fold and the number of countries with cases increased threefold thus justifying the decision.
On February 18, 2022, President Bidenproclaimed the Continuation of the National Emergency Concerning the Corona Virus Disease 2019 (COVID-19) Pandemic [FR Doc. 2022-03972].
On March 13, 2020, by Proclamation 9994, President Trump declared a national emergency concerning the coronavirus disease 2019 (COVID-19) pandemic. The COVID-19 pandemic continues to cause significant risk to the public health and safety of the Nation. For this reason, the national emergency declared on March 13, 2020, and beginning March 1, 2020, must continue in effect beyond March 1, 2022. Therefore, in accordance with section 202(d) of the National Emergencies Act (50 U.S.C. 1622(d)), I am continuing the national emergency declared in Proclamation 9994 concerning the COVID-19 pandemic.
On September 12, 2022, President Biden proclaimed Executive Order 14081 on Advancing Biotechnology and Biomanufacturing Innovation for a Sustainable, Safe, and Secure American Bioeconomy
Biden’s New Bio-Attack – Mother of All Bombs
Biden’s Mother of All Bombs transhumanistic genetic modification of everything (the Internet of the Body) is simply the psychotic desire to have aggressive remote control of all biological entities. Dementia Joe Biden, the current Big-Pharma White House agent, dropped his Mother Bomb on Americans on September 12, 2022, in an Executive Order (14081) entitled: Advancing Biotechnology and Biomanufacturing Innovation for a Sustainable, Safe, and Secure American Bioeconomy. This EO is another lost battle in Pharmaceutical WWIII. Fake president Biden has unleashed the transhumanists upon Americans without any restrictions, monitoring, or morality and given them unlimited funds to play with. The previous vaccines that delivered graphene oxide nanobots obviously weren’t enough for the depopulation mad-scientists, now they want to continue their genetic modifications unfettered, paid by the government, and with complete impunity. We know quite well that Big-Pharma lobbyists and lawyers write the Executive Orders and US Congressional laws concerning the medical industry and that politicians do not understand the ramifications at all. If they did understand, they could not vote for these demonic laws nor allow such industry-designed Executive Orders that act as administrative law within Federal agencies to be passed into US law. If politicians do understand what they voted for, they have committed treason and are complicit in mass murder – genocide through vaccines via the overthrowing of the US Constitution.
Biden’s puppet-masters learned long ago that presidential actions can create trillions of dollars in easy income for new vaccines, treatments, and drugs. His new Executive Order establishes the supremacy of drug companies in his new “bioeconomy” through “biotechnology”, and “biomanufacturing.” Pharmaceutical WWIII is an inhuman medical attack on the human bloodstream that is obviously planning to take over global eugenics as a money-making business. Biden has pulled out all the stops in this vague but sweeping attempt to empower Big-Pharma. This can be seen clearly in the Executive Order, once the verbiage is translated. The EO creates the National Biotechnology and Biomanufacturing Initiative which will control our lives even more than during Covid.
Biden’s EO is proof that the executive branch is now owned by the biomedical/pharmaceutical industry. Essentially, the transhumanists within Big-Pharma have completely taken over government policy and taxpayer funds to promote their own anti-human agenda of hacking the genetics of life and killing people in the process to advance depopulation. The mRNA injections are an experiment in transhumanism via vaccines. The genetic modification of all living things is anti-human and can only lead to more disaster and medical genocide. These poisonous vaccines, viral vectors, mRNA, and spike protein pathogen technologies are already inserted in many other vaccines, including flu shots, pneumonia shots, shingles, childhood vaccines, and numerous cancer treatments. The graphene oxide and SPIONS included as “inactive ingredients” in vaccines are toxic, mutagenic, and deadly to cells and tissue in the human body.
It is likely that this EO may have been timed in anticipation of the new pandemic treaty that the Biden administration is hoping to get passed through the United Nations World Health Organization. This treaty will transfer sovereignty over matters of “health emergencies” from the national level to the WHO with barely any possibilities for participating nations to reject the Organization’s dictates.
Biden’s Bioeconomy Provisions
Let’s take a look at some of the overtly anti-Constitutional provisions of Biden’s bombshell EO, with an accompanying translation into truth, instead of double-speak:
Section 1. Policy. It is the policy of my Administration to coordinate a whole-of-government approach to advance biotechnology and biomanufacturing towards innovative solutions in health, climate change, energy, food security, agriculture, supply chain resilience, and national and economic security.
We need to develop genetic engineering technologies and techniques to be able to write circuitry for cells and predictably program biology in the same way in which we write software and program computers; unlock the power of biological data, including through computing tools and artificial intelligence; and advance the science of scale-up production while reducing the obstacles for commercialization so that innovative technologies and products can reach markets faster.
Translation: This Frankenstein insanity is trying to “play God” – and that always goes bad. The graphene oxide “circuitry for cells” is toxic, mutagenic and has yet to be approved for use on humans due to cytotoxicity, gene damage, and the production of acidosis (cancer). Many treatments using graphene oxide in Biden’s new “biotechnology” are already being used without the FDA stopping the use of these deadly toxins.
(a) bolster and coordinate Federal investment in key research and development (R&D) areas of biotechnology and biomanufacturing in order to further societal goals;
(b) foster a biological data ecosystem that advances biotechnology and biomanufacturing innovation,
Translation: The biological data ecosystem refers to radio frequency ID chips, graphene neural net antennas, hydrogel transistors, and many other systems that are already in use. This “data” will be able to be read and controlled by external digital devices and will be the global “vaccine pass” written into “functionalize and templated superparamagnetic reduced graphene oxide polyethylene glycol nano-circuitry microchips” that will record all vaccinations and medical data for global governmental control of “medical safety and security.”
(c) improve and expand domestic biomanufacturing production capacity and processes, while also increasing piloting and prototyping efforts in biotechnology and biomanufacturing to accelerate the translation of basic research results into practice;
Translation: Permanent “Emergency Authorization Use Only” status is granted for all new diabolic vaccine experiments on humans and the inhuman medical nano-treatments that modify DNA, attack cellular functioning, and fill the body with man-made polymers derived from petroleum – like most pharmaceutical drugs. Animal studies will be skipped, and humans will be given shots and then studied for vaccine adverse events.
(d) boost sustainable biomass production and create climate-smart incentives for American agricultural producers and forest landowners;
Translation: Bioeconomy will take over all food production and turn it towards glyphosates and GMO seeds and plants. The BIO-LORDS will re-make humans, animals, PLANTS, and minerals through nanotechnological genetic manipulation.
(e) expand market opportunities for bioenergy and biobased products and services;
Translation: You will eat bugs and like it. Your body will be wirelessly connected to the grid and your bioenergy will be harvested. Your graphene oxide neural network will be added to the collective. Resistance is futile.
(f) train and support a diverse, skilled workforce and a next generation of leaders from diverse groups to advance biotechnology and biomanufacturing;
Translation: Lie, falsify, and propagandize psychopathic “bio-goals” as the best thing for safety and security, health and wellness, and quantum leaps in human evolutionary development; when they are simply devolution into automaton nano-programmed cyborg/robot transhumananist grotesque experiments that will ultimately fail miserably causing illness, tremendous harm, and death.
(g) clarify and streamline regulations in service of a science- and risk-based, predictable, efficient, and transparent system to support the safe use of products of biotechnology;
Translation: Throw out all regulations monitoring parasitical Big-Pharma vampirizing the world in an obvious effort to stop overpopulation.
(h) elevate biological risk management as a cornerstone of the life cycle of biotechnology and biomanufacturing R&D, including by providing for research and investment in applied biosafety and biosecurity innovation;
Translation: This means that bioweaponry research is now legal in America and Fauci and the NIH won’t have to pretend to farm in out to other nations through NIH grants. It also allows “gain-of-function bioweapon” research to be conducted under the guise of “biosafety and medical biosecurity.”
Sec. 5. Building a Vibrant Domestic Biomanufacturing Ecosystem.
Translation: Remove all hindrances to Big-Pharma continuing to control the world (bio-ecosystem) through medical fraud.
Sec. 7. Biotechnology and Biomanufacturing Workforce. (a) The United States Government shall expand training and education opportunities for all Americans in biotechnology and biomanufacturing.
Translation: Vaccine fascist control of “All Americans”, with no dissenters.
(ii) use Federal investments in biological sciences, biotechnology, and biomanufacturing to enterprise.
(iii) enhance cooperation, including joint research projects and expert exchanges, on biotechnology R&D, especially in genomics;
(iv) work to promote the open sharing of scientific data, including genetic sequence data
Translation: “Enhance cooperation” means steal all patents. “Promote open sharing” means maintain a complete monopoly. Big-Pharma will have unlimited citizen’s tax money to do whatever they want.
(j) The term “key R&D areas” includes fundamental R&D of emerging biotechnologies, including engineering biology; predictive engineering of complex biological systems, including the designing, building, testing, and modeling of entire living cells, cell components, or cellular systems;
Translation: We will turn you into transhuman enhanced cyborgs, and no one can stop us.
Frankenstein Biotechnology Atrocities
Graphene and its derivatives are emerging as a class of novel but versatile templates for the controlled preparation and functionalization of materials. Graphene is capable of acting as a low-dimensional hard template, where its two-dimensional morphology directs the formation of novel nanostructures. Graphene oxide and other functionalized graphenes are amphiphilic and may be seen as soft templates for formatting the growth or inducing the controlled assembly of nanostructures. In addition, nanospaces in restacked graphene can be used for confining the growth of sheet-like nanostructures, and assemblies of interlinked graphenes can behave either as skeletons for the formation of composite materials or as sacrificial templates for novel materials with a controlled network structure. Flexible graphene and its derivatives together with an increasing number of assembled structures (polyethylene glycol) show great potentials as templates for bio-materials production.
From: Frontiers, 15 March 15, 2022, Graphene Oxide and Biomolecules for the Production of Functional 3D Graphene-Based Materials
Graphene and its derivatives have been widely employed in the manufacturing of novel composite nanomaterials which find applications across the fields of physics, chemistry, engineering and medicine. Biomolecules and biopolymers have been extensively studied and employed during the last decade as building blocks, leading to the realization of graphene-based biomaterials owning unique properties and functionalities. In particular, biomolecules like nucleic acids, proteins and enzymes, as well as viruses, are of particular interest due to their natural ability to self-assemble via non-covalent interactions forming extremely complex and dynamic functional structures. The capability of proteins and nucleic acids to bind specific targets with very high selectivity or the ability of enzymes to catalyze specific reactions, make these biomolecules the perfect candidates to be combined with graphenes, and in particular graphene oxide, to create novel 3D nanostructured functional biomaterials. Furthermore, besides the ease of interaction between graphene oxide and biomolecules, the latter can be produced in bulk, favoring the scalability of the resulting nanostructured composite materials. Moreover, due to the presence of biological components, graphene oxide-based biomaterials are more environmentally friendly and can be manufactured more sustainably compared to other graphene-based materials assembled with synthetic and inorganic components for the fabrication of novel functional and scalable materials and devices.
PEGylation is Killing Us
From: Dovepress, Poly Ethylene Glycol (PEG) Functionalized Graphene Oxide in Tissue Engineering: A Review on Recent Advances, Ghosh S, Chatterjee K, April 21, 2020
Owing to the unique physical, chemical, mechanical and electrical properties, graphene and its derivatives have been extensively researched for diverse biomedical applications including in tissue engineering since the past decade. Tunable chemical functionalities of graphene oxide (GO), a graphene derivative, allow easy surface functionalization. Functionalization of GO with polyethylene glycol (PEG-GO) has received significant attention as it offers superior solubility, stability, and biocompatibility. Besides being an attractive candidate for drug delivery, PEG-GO can aid in the attachment, proliferation, and differentiation of stem cells, thereby augmenting tissue engineering. Cytotoxicity at large dosages and prolonged exposure of GO limits its clinical translation. Few studies have been reported on the use of PEG-GO in composite materials to prepare scaffolds for tissue engineering. However, these scaffolds incorporating PEG-GO for bone, cardiac, skin, and neural tissue engineering reveal promising outcomes.
PEG can be functionalized with different end groups so as to impart unique functionality to the nanoparticles when conjugated to GO. Ethylene glycol is one of several toxic alcohols that have medical and toxicological importance; if untreated, ingestion of ethylene glycol can be fatal. PEG containing acrylate groups can be incorporated in photo-curable bioinks for 3D printing of tissue scaffolds. Long-term effects of implanting scaffolds incorporating PEG-GO for tissue regeneration are poorly understood. PEG-GO is poised to emerge as a choice of biomaterial for advanced tissue engineering applications.
The possibility to obtain well-orchestrated polymeric architectures represents an emerging field of materials science for the development of advanced materials, including drug delivery devices, mimics of biological tissues, nanoreactors, and multifunctional coatings. Graphene oxide (GO) is a promising filler for polymer nanocomposites. GO is known to possess tunable physical-chemical characteristics, including optical, electrical, mechanical, antimicrobial properties, biocompatibility, UV-blocking, catalytic activity, and affinity to a wide range of pollutants. It can be easily reduced into graphene or chemically modified, thus holding promising potential as a versatile building block for the realization of nanostructured devices.
Many studies have reported on the preparation of nanocomposites achieved via incorporation of GO inside the polymer matrix, and surface functionalization of flexible substrates. Prospects of gathering the unique properties of this nanomaterial with the ease of processability and free-standing properties of polymers into a lightweight devices via GO-coating of polymers finds application in an extremely wide range of fields, including nerve tissue engineering, electronics, water treatment, sensors, energy storage, covalent binding, vacuum filtration-aided coating, dip-coating, and spray-coating.
From: Advanced Engineeering Materials, 2017, (#19, 1700627), Graphene Oxide/Polymer-Based Biomaterials, by Duygu Ege, Ali Reza Kamali, and Aldo R. Boccaccini
Since its discovery in 2004, derivatives of graphene have been developed and heavily investigated in the field of tissue engineering. Among the most extensively studied forms of graphene, graphene oxide (GO), and GO/polymer-based nanocomposites have attracted great attention in various forms such as films, 3D porous scaffolds, electrospun mats, hydrogels, and nacre-like structures. In this review, the most actively investigated GO/polymer nanocomposites are presented and discussed, these nanocomposites are based on chitosan, cellulose, starch, alginate, gellan gum, polyvinyl alcohol, polyacrylamide, polye-caprolactone (PCL), polylactic acid, pol(lactide-co-glycolide, gelatin, collagen, and silk fibroin.
With the addition of GO, the mechanical performance of GO composites were extensively improved under physiological conditions. GO/polymer-based scaffolds can be categorized into four main categories, namely, 3D porous scaffolds, electrospun mats, hydrogels, and nacre-like structures. Electrospun mats were produced for different types of applications including bone, neural, muscle, and skin tissue engineering. GO/polymer hydrogels have been mainly prepared for soft tissue engineering such as wound dressing, peripheral nerve regeneration, and muscle tissue engineering. Hydrogels with higher mechanical strength such as crosslinked GO/PVA also show potential for load-bearing applications such as articular cartilage regeneration.
From: MedScape: Practice Essentials
Ethylene glycol is used in PEG (ylation) and is one of several toxic alcohols that have medical and toxicological importance; if untreated, ingestion of ethylene glycol can be fatal. Although propylene glycol is a commonly used solvent for intravenous medications, it becomes toxic when administered in large doses over a short period. Iatrogenic propylene glycol can cause the following: hyperosmolality, anion gap metabolic acidosis, acute kidney injury, multisystem organ failure, refractory hypotension, arrhythmias, hemolysis, renal dysfunction, seizure, coma, CNS depression and seizures. Ethylene glycol’s toxicity mainly results from the accumulation of its toxic metabolites. Ethylene glycol is a central nervous system (CNS) depressant that produces acute effects similar to those of ethanol. These CNS effects predominate during the first hours after exposure. If undetected or untreated, ethylene glycol ingestion can cause serious or fatal toxicity.
The main toxicity of ethylene glycol results from hepatic metabolism of ethylene glycol to glycoaldehyde, glycolate, glyoxylate, and oxalate. These metabolites inhibit oxidative phosphorylation and cellular respiration, glucose and serotonin metabolism, protein synthesis, DNA replication, and ribosomal RNA formation. Other effects include CNS depression and cardiopulmonary and renal failure. The accumulation of organic acid metabolites, especially glycolic acid, results in an elevated anion gap metabolic acidosis.
The following severe cardiovascular effects have been reported in persons 12-24 hours after ingesting ethylene glycol: Hypertension or hypotension, Dysrhythmias (from electrolyte abnormalities), Congestive heart failure with cardiogenic pulmonary edema, Circulatory collapse, Cardiac arrest, and Death.
The initial phase of ethylene glycol poisoning in humans is characterized by inebriation caused by unmetabolized ethylene glycol. The following effects are common in acute poisoning cases:
Ataxia, Slurred speech, Drowsiness, Irritation, Restlessness, and Disorientation. Possible consequences of neurologic effects in severe poisonings include the following: Myoclonic jerks, Convulsions, Coma, and Death. Cerebral edema and deposition of calcium oxalate crystals in the walls of small blood vessels in the brain contribute to this CNS toxicity. Some studies have documented brain dysfunction with corresponding cranial computed tomography (CT) findings after ethylene glycol ingestion, such as low-density areas in the basal ganglia, thalami, midbrain, and upper pons.
According to some investigators, effects on cranial nerves appear late (generally 5–20 days after ingestion) and constitute a fourth, late cerebral phase in ethylene glycol. The following cranial nerve effects have been reported after acute exposure: Facial palsy, Hearing loss, Dysphagia, Ophthalmoplegia, and Visual disturbances.
Inhaled ethylene glycol can irritate the respiratory tract. Throat and upper respiratory irritation were the most common complaints after prolonged experimental exposures in humans. Exposure to 60 ppm aerosolized ethylene glycol caused noticeable respiratory irritation. Exposure to 80 ppm aerosolized ethylene glycol was “intolerable” because respiratory discomfort developed rapidly. Pulmonary edema, adult respiratory distress syndrome (ARDS), and death have occurred in persons exposed to ethylene glycol. The following respiratory effects often occur 12 hours or more after exposure in victims of severe ethylene glycol poisoning: Tachypnea, Hyperventilation, Kussmaul respirations, and severe metabolic acidosis.
Ethylene glycol victims revealed the following: Pulmonary edema with diffuse hemorrhagic exudates, Bronchopneumonia, Deposits of calcium oxalate crystals in lung parenchyma. Nephrotoxicity after ethylene glycol ingestion typically occurs 24-72 hours after acute exposure. Nausea, vomiting, and abdominal pain often occur soon after ethylene glycol ingestion. Also, leukocytosis, methemoglobinemia, and bone marrow arrest. Reported musculoskeletal effects have included: muscle tenderness and elevation of creatine kinase.
Ethylene glycol exposure was teratogenic to mice and rats, resulting in craniofacial and neural tube closure defects and skeletal dysplasia. Oral doses of ethylene cause developmental toxicity in those animals, including: axial skeletal malformations, reduced body weights, external malformations, and increased post-implantation loss.
The Battle Between Light (Photons) and Dark (Graphene)
Photomedicine is a type of biotechnology that specializes in the therapeutic application of light – “light medicine.” It uses non-ionizing electromagnetic radiation in dermatology, oncology, surgery, radiology, DNA manipulation, and diagnostics. The fundamental particle of light is referred to as a photon. Photons are both a particle and a wave. They are deemed to carry no charge and have no mass. In a biological system, photons are emitted when electrons move from one energy state to another. Photomedicine is used to treat various conditions, such as tissue injuries, psoriasis, seasonal affective disorder, and other circadian rhythm disorders, cancer and tumors, and alopecia.
Weak emission of light from cells in a living organism were discovered by the Russian embryologist Alexander Gurwitsh in 1926, who called them mitogenetic rays. Half a century later, the German researcher Fritz Albert Popp, a Nobel Prize nominee in Physics, re-confirmed their existence and established the term biophoton. Popp experimentally demonstrated that dozens of photons of light are emitted every second from every square centimeter of biological area. Popp proved that biophoton emission is not confined to thermal radiation or bioluminescence.
Diagnostic photomedicine involves the use of light for various imaging technologies, e.g. X-ray, MRI, and PET. Other forms of photomedicine include photodynamic therapy (PDT), low-level laser therapy (LLLT), and LED therapy. Photodynamic therapy (PDT) is a treatment that involves light-sensitive medicine and a light source to destroy abnormal cells. It can be used to treat some skin and eye conditions, as well as certain types of cancer.
Photodynamic therapy can be used to treat abnormal cells in parts of the body that a light source can reach, such as the skin, eyes, mouth, food pipe, esophagus, and lungs. Common conditions treated with PDT include: actinic keratoses, Bowen’s disease, basal cell carcinoma, macular degeneration, esophageal cancer, mouth cancer, lung cancer, warts, acne and Paget’s disease.
When some photomedicines are exposed to the light, they activate and cause a reaction that damages nearby cells. This allows small abnormal areas of tissue to be treated without the need for surgery. Infrared light can heal cells and tissue while ultraviolet kills cells and tissue and is particularly effective at “turning off” targeted genes with the use of luciferase and luciferin. Bioluminescence is the outcome of the oxidation of luciferin and the enzyme luciferase. This is exemplified by bioluminescent organisms such as the firefly. Using light to turn DNA on and off effects the fields of DNA biotechnologies, synthetic biology, and epigenetics.
After several independent studies demonstrated that living cells do not just radiate light, they also absorb light, scientists are now investigating the existence of a new form of communication using light. Biophotons could offer that supplementary signaling pathway next to electrical and chemical pathways for intra- and intercellular communication. It is known that photosensitive biomolecules of cells and neurons can absorb biophotons and transfer the absorbed biophotons energy to nearby biomolecules by resonance energy transfer, which can induce conformation changes and trigger complex signal processes in cells and between cells. Indeed, hollow microtubules with constant inner diameters inside the brain could act as optical fibers for biophoton transmission within brain nerve cells. A significant relationship between the fluctuation function of microtubules due to biophotons emission and alpha-EEG has been detected.
It has been suggested that the major source of biophotons is the DNA. The first supporting fact is that cells emit biophotons even when the cytoplasm is damaged, however when the nuclei is removed, biophoton emission stops. Red blood cells, which have no active chromatine (DNA) are the only cells which do not emit biophotons. The mechanism of biophoton absorption, storage and emission is however not well understood.
Photomedicine has been particularly effective at regenerating frayed DNA telomere. This ability for DNA repair indicates the possible medicines of the future. Some of the most effective pain relief comes from application of LED light, infrared light, and laser light directly to the effected area. These devices are over-the-counter “light medicine.” In effect, light heals and the use of light-absorbing graphene oxide, in all of its forms, kills.
Enter the Battle
Whether we want it or not we are in the midst of a life and death battle for our own bloodstream. The enemy has the high ground, the money, the controlling infrastructure and a host of evil bioweapons disguised as safe and secure “medicines.” Iatrogenic death is considered by many to be the number one cause of death in America – doctor and drug induced death. The medical industry is one of death, not life. We are all in the cross-hairs of Big-Pharma who overtly claim that six billion people need to die, soon. The above article indicated the methods of delivery and the bombs they are using to cull humanity world-wide. But, darkness can’t see very far into the future because humans are extremely unpredictable and most do not consciously wish to turn to the dark side.
Fortunately, it is “light medicine” that may be the answer to dispelling the darkness of medical fake-science that has humanity in a death-grip. It has often been said in many religions, myths, and belief systems – light will win the day and dispel the darkness. Just turn on the light of consciousness and gain the gift of discernment to guide you through this vale of darkness and misery created by doctors, scientists, and politicians. Then, the light of a new day will dawn, and the dawn-treaders and forerunners will lead us to a new science of medicine based, literally, on light and love.
Let’s take another look at Candace Owen’s father-in-law who turns out to be head-dog in the Queen’s global gold and silver futures rigging business. Listen and learn as anyone, with the “right” connections can earn billionaire bucks off this precious metals rigging scheme that would make Charles Ponzi proud.
Shocking details inside link below:
Candace Owens’ new father-in-law, Baron Michael Stahel Farmer, has controlled the gold, silver, metals, oil, trading, communications (propaganda) and now carbon credits markets for 50 years.
Lord Farmer, who now spouts Christianity, is likely Khazarian Jewish, German and Sabbatean-Frankist (sin with abandon) like the Rothschilds, if not in fact, then by interlocked association.
We believe Lord Farmer facilitated the ENRON false flag to consolidate ICE FUTURES exchanges* in London and gave control of gold & silver to JPMorgan Chase which since inception in 1799 has always has been a Rothschild–Alexander Hamilton (British Spy #007) creature.
Next time Candace is receiving questions from her audience or you have an opportunity to ask her an online questions, inquire about her husband’s relationship to the Pilgrims Society, George Soros, and silver/gold rigging. If she doesn’t know, then it is true – her head is as empty as her American patriotism .
This article will address some of the following questions:
Is there a diabolical plan behind superparamagnetic graphene/iron oxide nano-particles that are being found in the bloodstreams of people who have received the Covid vaccine or died from Sudden Adult Death Syndrome?
Could the super-permeation of graphene family substances in food, drinks, water, vaccines, medicines, cosmetics, packaging, and medicines be a planned conspiracy against human health?
Are graphene oxide “circuits” being created in the human body to control the many nano-particle metals being injected into people through vaccines and through the ingestion of food?
Can graphene oxide be “pre-programmed” before being inserted into injections, food, and the environment?
Is the transhumanistic plan for “aggressive remote-control of all things” (Internet of Things, Internet of the Body) actually possible through new scientific “mad-scientist” experiments of human subjects using the Graphene Family Nano-materials?
Throughout the world, doctors are putting the Covid vaccine under the microscope, along with human blood from vaccinated people, and discovering the most astoundingly disgusting results that prove that pharmaceutical companies are lacing jabs with nano-metals, graphene and iron oxide nano-structures, and many other substances of “unknown” origin. These substances are accumulating in blood vessels as they self-organize and self-replicate with the magnetic and electrically conductive materials found in the vaccines that are being used by the pre-programmed graphene oxide to build unidentifiable structures in blood vessels and tissue that block blood flow creating strokes and heart attacks. These “structures” have also been analyzed and found to contain the same substances.
Graphene oxide “quantum dots”, also called “evil dust”, jumps over the brain-blood barrier and deposits toxic Graphene Oxide in the mid-brain, causing Alzheimer’s and Parkinson’s like symptoms – also called human spongiform encephalitis. Graphene Oxide flakes, sheets, webs, and 3D structures build blood clots that create vascular obstructions and heart problems leading to the “vaccine death” now called Sudden Adult Death Syndrome. Many of these new illnesses and symptoms are caused by, or exacerbated by, Graphene Oxide substances that “build” unwanted, and unnatural structures in the human body that are foreign, man-made, sub-natural substances causing toxicity, harm, and death. Graphene Oxide organizes nano-metals into circuits that become sensors, activators, antennas, broadcasters, magnetic triggers, bio-electric devises, and mechanisms for diagnostic feedback in magnetic resonance imaging. A doctor can take readings from these circuits with external devises.
Unfortunately, these mad-scientific, immoral research projects got out-of-hand during the fake pandemic when all safety protocols were ignored. Humans are now the lab rats for vaccine gain of function bioweapon experimentation without any consideration for adverse vaccine reactions. Of course, the bigger question is: Why did the CDC, NIH, WHO, Congress, Courts and the President sanction these crimes against humanity? Sadly, the answer is that this is Standard Operating Procedure for Big Pharma that is actually not an industry of health, but one of promoting illness and death – a pharmaceutical killing-field of depopulation. It is easy to understand why so many people believe that Big Pharma is a depopulation syndicate of rich elite who wish to decrease the Earth’s population by billions of people – and, as quickly as possible without being noticed and with complete impunity. Sadly enough, there seems to be no other answer than the fact that this is all a planned eugenics policy of transnational pharmaceutical (vaccine) syndicates aligned with Big Pharma, WHO, CDC, NIH and many other agencies and organizations.
First, let’s take a look at the proof that this toxic poison is in the bodies of vaccinated people via microscopic examination. It is important to remember that most Covid vaccinations have these graphene/iron oxide “adjuvants” in them, especially childhood vaccines since 2008, flu shots, shingles and pneumonia vaccinations, as well as many medical treatments and procedures.
Hundreds of doctors worldwide are now examining the Covid vaccines, and human blood samples, under microscope and finding results that seem to be from a horrifying science-fiction movie.
In an article from The Defender, on August 25, 2022, entitled, Toxic, Metallic Compounds Found in All COVID Vaccine Samples Analyzed by German Scientists, by The Epoch Times, Enrico Trigoso:
A group of independent German scientists found toxic components – mostly metallic – in all the COVID-19 vaccine samples they analyzed, “without exception” using modern medical and physical measuring techniques. The Working Group for COVID Vaccine Analysis says that some of the toxic elements found inside the AstraZeneca, Pfizer, and Moderna vaccine vials were not listed in the ingredient lists from the manufacturers. The following metallic elements were found in the vaccines:
Alkali metals: caesium (Cs), potassium (K)
Alkaline earth metals: calcium (Ca), barium (Ba)
Transition metals: cobalt (Co), iron (Fe), chromium (Cr), titanium (Ti)
Rare earth metals: cerium (Ce), gadolinium (Gd)
Mining group/metal: aluminum (Al)
Carbon group: silicon (Si)
Oxygen group: sulphur (S)
“We have established that the COVID-19 vaccines consistently contain, in addition to contaminants, substances the purpose of which we are unable to determine,” their study says.
In an article from The Expose entitled: Covid Injection Aftermath: Study finds 94% of “Vaccine” Recipients have Pre-Blood Clot Formations and Foreign Particles, by Rhonda Wilson, on 8/24/2022 the author states: “An Italian study published two weeks ago in the International Journal of Vaccine Theory, Practice, and Research revealed almost everyone who had been injected had abnormalities after Covid vaccination. In 94% of vaccinees’ blood, there was an aggregation of red blood cells and the presence of particles of various shapes and sizes. The study began in March 2021. Using dark-field microscopy, the researchers analyzed blood samples from 1,006 referred to the Giovannini Biodiagnostic Centre for various disorders after being injected with Pfizer/BioNTech or Moderna mRNA vaccines.
In the study, authors noted that the vaccines are purported to contain at least the spike protein from SARS-CoV-2 but are known also to contain foreign particles. “Among those foreign components are metallic objects as demonstrated previously in this journal by Lee et al. (2022) which are confirmed in our results.” Of the 1,006 cases analyzed, only 58 – equal to 5.77% of the total – presented a completely normal hematological picture upon microscopic analysis after the last mRNA injection with either the Moderna or Pfizer vaccine. The blood of 948 – 94% of the study’s participants – showed aggregation of red blood cells and the presence of particles of various shapes and sizes of unclear origin one month after the mRNA injection.
Blood clots found by morticians have been sent all over the world to be studied by independent teams. The only thing that is for sure is that something is taking the injected metals and building them into “killer clots” throughout the body. These clots have substances and structures inside of them that are “unidentifiable” and cannot be explained by anyone. But they are obviously designed to kill the host body that receives the injections.
Graphene Oxide flakes self-organize, move towards each other, and build layers like an independent robot. That is why they are used in hydrogels for the slow release of medicine in a patch, a patch that can sense what the Graphene Oxide receivers are broadcasting about the chemical function of the liver, pancreas, or most any other diseased area. A doctor can also read a Graphene Oxide “infested” organ and then give electrical/magnetic commands for a hydrogel to release a specific amount of medicine. Graphene Oxide (GO) can do wonders because it is monoatomic – one atom thick, either as a “dot”, “flake”, “sheet”, “tube”, “web”, or “buckyball/fullerene.” Graphene is carbon and carbon is the source of organic processes because it is seemingly amorphous, like silica in the inorganic world. As GO sheets, GO hyper-connects in all directions (superconductivity) in length and breadth and scientists say it is 2D – which it is not. Even though, a sheet of GO is transparent, electro-conductive, 100 times stronger than steel, self-organizing, and self-replicating when in the presence of specific EMFs and magnetic fields. Graphene Oxid, GO, can be the scaffolding for just about anything, organic or inorganic.
Graphene Oxide as nano-tubes has created a diabolic industry of nano-technology that is far more evil than most people are aware of and yet touches most aspects of their life through myriad industries beyond just medical uses. Graphene Oxide and iron oxide (both superparamagnetic) are everywhere, but especially in vaccines, medicines, and food. They supposedly control and target vaccine delivery but are also known for being a common adjuvant, a substance that is seen as “foreign” (xenobiotic/inhuman) that creates an immune reaction because it is seen as an antigen or pathogen trying to harm the body. Graphene Oxide is considered toxic (cytotoxic) in the smallest amounts and accumulates in the body and yet it is used everywhere, including the lipid-coated nanotubes that deliver vaccines and other medicines. It is also mutagenic, causing DNA damage and continuing mutation, just as mRNA vaccines have recently been proven to do.
Graphene Oxide as nanowebs can combine dots, flakes, tubes, and sheets into animated nanowebs that self-organized, self-replicate and direct the building of tissue-like material in the circulatory system, as well as nanocircuits that target certain organs (brain, heart, ovaries, testes, liver, etc.) and carry the payload inside the nanotube to the targeted organ. All of these things are already happening, these are not science predictions, they are science fact. These types of inhuman, mechanical, anti-life systems are being used right now, approved by the FDA, CDC, NIH, WHO, AMA, etc., to target and attack cancer cells in a variety of organs. Doctors can inject and move large amounts of Graphene Oxide with a magnet to a specific organ, inject a hydrogel and control the release of more nano-tubes from the hydrogel with a phone app to conduct telemedicine. These GO nan-technologies, merged with mRNA, create the most-deadly genocide in human history because we have only seen the initial results. Some estimates are that over twelve million have died directly associated with the current jab. Untold others have terrible adverse reactions. That doesn’t take into consideration the millions who have died due to the same vaccine death shots given out continuously for flu, pneumonia, shingles, or childhood vaccines. The vaccine induced Sudden Infant Death Syndrome is now joined by the Sudden Adult Death Syndrome and the medical authorities actively look the other way as hundreds of athletes drop dead on the playing field before the audience. And still, the vaccine has not been pulled from the market and the guilty prosecuted.
Graphene Oxide as fullerenes (buckyballs) is, as yet, little used. It is a man-made 3D structure folded from GO sheets which can also make other 3D geometric solids. This is totally different than C-60, a natural occurring substance which is presumed to be from meteorites. Naturally occurring C-60 (fullerenes/buckyballs), which can be found in the rare mineraloid shungite, has nothing to do with the GO buckyballs created in laboratories. Scientists believe that bucky-balls (C-60) originate in space and are a highly developed form of carbon exposed to cosmic heat. There is also C-70, C-80, and other carbon compounds found in space that have exposed carbon to tremendous heat, which is one way to create Graphene Oxide – burn a steak on your barbeque and you have simple Graphene Oxide.
It seems quite likely that as human intelligence develops, so too does carbon develop in its many organic forms through a natural process of metamorphoses. We owe our life to carbon and if more perfect forms of carbon already exist in our solar system and cosmos, then obviously we can metamorphose carbon into higher forms and functions. Unfortunately, our voodoo witch-doctor mad-scientists haven’t considered any of these ideas as they are actively devolving into a “Graphene World” of one, two, and three dimensional, man-made monstrosities by injected a Frankenstein mutation (mRNA is mutagenic) into the new Graphene Oxide, Genetically Modified Human Being, a new species that has fallen out of the 3D world into the 2D Graphene World. Humans can advance to an objective view of time and enter a world of spiritual endurance (4D) instead of the illusion of linear time (3D). Modern materialistic science has devolved into two dimensional nanowebs that mimic human neural nets with 2D nanosheets/nanowebs that build “fake” human tissue with their 1D nano graphene dust/graphene flakes that are designed to kill human beings, ultimately leading to 0D – death. This is clearly planned elimination of everyone who does not know the secret – “Don’t take any injections of any kind.”
Graphene World is a world of sub-nature, a step backwards into immoral animal, plant, and mineral realms, not a step forward into higher forms of carbon in super-nature that are part of human ascension. Graphene Oxide is a man-made sub-element that can only lead into darkness and the horrifying medical genocide we are seeing around us in all fields of medicine. Every person involved in gain of function research on deadly viruses and vaccines is an enemy to humanity. Using GO to deliver any vaccine is diabolical, then add mRNA and you have a truly evil group of murderers. These types of experiments on “uninformed” humans are creating a new species of ill and dying humanity and an elite pharmaceutical syndicate that openly advocates depopulation by injection, toxic food, toxic chem-trail air, a medical industry creating illness, economic slavery, psychological subliminal programming, and the mass hypnosis of media propaganda that sold the world a fake pandemic – the fear of Virus X. Virus X, the highly prophesied pandemic of huge proportions, is spliced into the synthetic virus that was created in a bioweapon P-4 labs and disseminated to all other P-4 secure biolabs throughout the world. This biological weapon of mass destruction was bio-engineered with funding from Dr. Anthony Fauci and the National Institutes of Health, the CDC, and the World Health Organization of the United Nation. The United Nations is a clear Anti-American war-actor that took over American Constitutional freedoms via Pharmaceutical Terrorism with a fake pandemic supported with lies and bad protocols that killed millions. It was made possible by Congress passing laws that allowed it: The All Hazards and Pandemic Act of 2019.
Iron oxide as a vaccine adjuvant has been in most childhood vaccines since 2008. Graphene Oxide is present everywhere in the environment and yet is poisonous, as proven in every study of its toxicity. And yet the medical industry pushes forward without any moral reflection on the harm being done to humans. These Big Pharma doctors and drug-pushers are individuals who have devolved into immoral animals who are now below even what an animal would do to another animal. The demonic forces involved in this global Pharmaceutical World War III are quite real and wish to turn all humans into machine-augmented cyborgs who can be “stopped” or “controlled” by pushing a button that activates transhuman wetworks inside the human body. This nefarious plan has been patented by Richard C. Walker and is called “The Aggressive Remote Control of Everything”, which can only be fully accomplished by having an “OFF” button on every human being created by nano graphene technology.
Graphene Oxide (GO) is a single atom carbon layer where both surfaces of the layer are modified by oxygen containing functional groups that are bonded together in a repeating pattern of hexagons. There is tremendous interest in graphene and its derivatives [graphene oxide (GO) and reduced GO (rGO)] due to their superior mechanical, thermal, electrical, optical, and chemical-adsorption properties. In the past few years, graphene-based materials attracted much attention and were used for many practical applications in various industries. Recent developments on graphene synthesis from foodstuffs, use of graphene for food analyses, and graphene-based analytical methods in detection (e.g., composition, contaminants, toxins, and volatile organic compounds) are used to help to ascertain the quality and/or safety of foods. There are also antibacterial properties of graphene-based nanomaterials and their applications in food packaging.
Graphene Family Nano-materials trigger local and systemic toxic effects, induce genotoxicity in vitro and in vivo, alter the gut microbiome, cause genetic mutations, and are inedible. Further toxicological and risk assessment studies are needed especially when used in food or injections of any type.
Different applications have been suggested for graphene nano-materials (GFNs) in the food and feed chain. However, it is necessary to perform a risk assessment before they become market-ready, and when consumer exposure is demonstrated. For this purpose, the European Food Safety Authority has published a guidance that has been recently updated to identify and characterize toxicological hazards related to GFNs after oral exposure. GFNs seemed to resist gastrointestinal digestion and were not able to be absorbed, distributed, and excreted, inducing toxic effects at different levels, including genotoxicity. Also, dose has an important role as it has been reported that low doses are more toxic than high doses because GFNs tend to aggregate in the digestive system, changing the internal exposure scenario. Thus, further studies including a thorough toxicological evaluation are required to protect humanity from the, as yet unknown, effects of GFNs.
Although Graphene Oxide – like graphene – is also a 2 Dimensional material, its properties are very different from that of graphene. It does not absorb visible light, has a lower electric conductance compared to that of graphene, and demonstrates significantly higher chemical activity. Its high electron mobility is 100x faster than silicon; it conducts heat 2x better than diamond; its electrical conductivity is 13x better than copper; it absorbs only 2.3% of reflecting light; it is impervious so that even the smallest atom can’t pass through a defect-free monolayer graphene sheet with a thickness of about 0.33 nanometers. There are about 3 million layers of graphene in a 1 mm thick sheet of graphite. Harder than diamond yet more elastic than rubber; tougher than steel yet lighter than aluminum – graphene is the strongest known material.
Some of the most promising applications of graphene are publicized as being in electronics (as transistors and interconnects), detectors (as sensor elements) and thermal management. The first graphene field-effect transistors (FETs) have already been created and used for nano analog communication or nano digital applications.
An ever-increasing number of research groups are exploiting programmable self-assembly properties of nucleic acids in creating rationally designed nano-shapes, nano-machines, and nano-electronic devices that can self-assemble for many different uses. These devices include nano-routers, nano-antennas, and nano-circuit boards. Medical nano-technology researchers have created nano-bots, a popular term for molecules with a unique property that enables them to be programmed to carry out a specific task.
When Graphene Oxide is injected into the body and interacts with biological blood or tissue, the GO picks up hydrogen and becomes graphene hydroxide. The OH (hydroxy) groups can then split off a proton which leaves a negative charge affecting the whole graphene sheet and making it highly acidic and damaging to red blood cells. It also is incredibly sharp and acts like razor blades cutting blood vessels, tissue, and organs. Self-organizing GO tubes and sheets can block capillaries and arteries, with devastating effects when this occurs in the heart and lungs.
Graphene Oxide inside the body causes thrombogenicity, blood clotting, post inflammatory syndrome or systemic or multi-organ inflammations, causes alteration of the immune system, collapse of the immune system, cytokine storms, neurodegeneration, and mutagenic effects changing the DNA of the host. Inhaled Graphene Oxide spreads evenly throughout the alveolar tract and causes bilateral pneumonias, inflammation of the mucous membranes, and loss of taste and smell. Graphene Oxide toxicity in the human body behaves like SARS-CoV-2, generating the same symptomatology.
Graphene, Graphene Oxide (GO), carbon nano-tubes, and the entire graphene-family nano-materials (GFN) are toxic in almost all their forms, causing mutagenesis (cancer, chromosomal alteration), cell death, apoptosis, necrosis, and the release of free radicals. It creates immunosuppression, damage to the central nervous system, circulatory, endocrine, reproductive, and urinary systems, which can cause anaphylactic death, and multi-organ dysfunction. It increases toxicity rapidly in the lungs, creating cytokine storms leading to bilateral pneumonia, genotoxicity, and DNA damage.
Several typical mechanisms underlying Graphene Oxide nano-material’s toxicity have been revealed in numerous studies, for instance, physical destruction, oxidative stress, DNA damage, inflammatory response, apoptosis, autophagy, and necrosis. In these mechanisms, toll-like receptors, transforming growth factor-beta (TGF-β) and tumor necrosis factor-alpha (TNF-α) dependent-pathways are involved in the signaling pathway network, and oxidative stress plays a crucial role in these pathways. Many experiments have shown that Graphene Oxide nano-materials have toxic side effects in many biological applications. According to the USA FDA, graphene, Graphene Oxide, and reduced graphene oxide elicit toxic effects both in vitro and in vivo. Graphene-family nano-materials (GFN) are not approved by the USA FDA for human consumption.
Graphene Oxide has been used in a wide variety of nano-medical applications including tissue engineering, cancer treatment, medical imaging, and drug delivery. Its physiochemical properties allow for a structure to regulate the behavior of stem cells, with the potential to assist in the intracellular delivery of DNA, growth factors, and synthetic proteins. Due to its unique behavior in biological environments, GO is used in cancer therapies. It has also been used in vaccines and immunotherapy, including as a dual-use adjuvant and carrier of biomedical materials. In September 2020, researchers at the Shanghai National Engineering Research Center for Nanotechnology in China filed a patent for use of Graphene Oxide in a recombinant vaccine under development against SARS-CoV-2.
The properties of graphene are exceptional from a physical, thermodynamic, electronic, mechanical, and magnetic point of view. Its characteristics allow it to be used as a superconductor, crystallized graphene nano-antenna, and graphene quantum dot nan-orouters. It is an electromagnetic wave absorbing material, a signal emitter-receiver, and an antenna which makes it possible to create advanced nano and micrometric scale electronics. Graphene is a radio-modulatable nano-material. The graphene molecule also has the ability to inject electrons into other biological substances depending on the electromagnetic environment and temperature. Graphene is activated at room temperature and above.
Graphene can multiply radiation, acting as a nano-antenna, or else a signal repeater, a transistor. Exposure to electromagnetic radiation can cause the exfoliation of the material into smaller particles called Graphene Quantum Dots (GQD), whose properties and physical peculiarities are enhanced since they act by amplifying electromagnetic signals and, with that, the emission distance, especially in environments such as the human body. Graphene quantum dots can acquire various morphologies like hexagonal, triangular, circular, bucky-bulls, or irregular polygons and geometric solids.
The nightmare of Graphene Oxide circuits in human food is a Frankenstein monster that kills. As Mark Wilson’s headline reads: Edible Graphene Is Here, And Electronics In Your Food Are Coming. Mark’s article highlights the research conducted by Jeff Fitlowfrom Rice University thatuses a stock laser to carve edible circuits into food. These researchers have successfully used a commercial laser to transform the surface carbon in foods – like toast, coconuts shells, potatoes, and Girl Scout cookies – into graphene. Without using any special vacuums or clean rooms, graphene can be patterned into an impossibly thin, edible circuit. Graphene can be used to help fuel cells to store power, radio hardware to transmit data, glowing elements to light up, and all sorts of sensors, as well as deliver a preprogrammed piece of toast that can control your body. These graphene circuits resemble a dark, inky tattoo, a bit like very burnt toast. But, don’t forget, graphene is inedible, toxic, and a nerve poison.
Iron oxide nano-structures (IONs) in combination with graphene or its derivatives – e.g., Graphene Oxide and reduced graphene oxide – hold great promise toward engineering of efficient nano-composites for enhancing the performance of advanced devices in many applicative fields. Due to the peculiar electrical and electrocatalytic properties displayed by composite structures in nanoscale dimensions, increasing efforts have been directed in recent years toward tailoring the properties of IONs-graphene based nanocomposites for developing more efficient electrochemical sensors.
Unique features of IONs e.g., strong magnetic properties, low toxicity, high adsorption ability for immobilization of desired biomolecules and good biocompatibility, together with elegant properties of this new member of the carbon family e.g., high electrical/thermal conductivity, large surface area and electrocatalytic properties, have stimulated many interests for overcoming difficulties in realizing new scientific ideas or improving the performance of many current devices and methods. Catalytic activity of the graphene-IONs can be improved due to enhanced electronic communication e.g., charge transfer between catalyst and support. Additionally, synergistic effects of graphene sheets and IONs components provide nano-composite with novel physicochemical properties and consequently enhance electrochemical performance. As a result, graphene-IONs nano-composites have been considered as one of the most promising hybrid materials that can boost the development of more efficient electrochemical sensors.
Due to their tissue-like mechanical properties, hydrogels are being increasingly used for biomedical applications; a well-known example are soft contact lenses. These gel-like polymers consist of 90 percent water, are elastic and particularly biocompatible. Hydrogels that are also electrically conductive allow additional fields of application, for example in the transmission of electrical signals in the body or as sensors. Graphene and graphene derivatives (e.g., Graphene Oxide (GO) reduced graphene oxide (rGO)) have been incorporated into hydrogels to improve the properties (e.g., mechanical strength) of conventional hydrogels and/or develop new functions (e.g., electrical conductivity and drug loading/delivery). Unique molecular interactions between graphene derivatives and various small or macromolecules enable the fabrication of various functional hydrogels appropriate for different biomedical applications. In order to produce electrically conductive hydrogels, conventional hydrogels are usually mixed with current-conducting nano-materials that are made of metals or carbon, such as gold nano-wires, graphene or carbon nano-tubes.
To demonstrate the truth and efficacy of the above statements concerning the graphene family materials, we present below a series of research projects which summarize the “state of the art” concerning research in Graphene Oxide in its many forms. Much of what has been said above may have sounded alarmist, or even like wild, sci-fi fairytales of transhumanism, but the research below demonstrates that all of the experiments on humans with graphene substances has been going on for many years on a massive scale. The “innovations” in nano-particle research are not “illegal” but should certainly be “not allowed” by any moral scientist, doctor, or sane person. For the sake of innovation, humanity is now a collective lab rat to be experimented on by morally bankrupt drug-doctors preaching the Gospel of Transhuman manipulation of the building blocks of DNA, human organs, tissue creation, neurological control through wetworks, and inhuman mechanical thinking that dominates “precision medicine” and nano-biology. Essentially, nano-biology should be an oxymoron instead of the current medical, experimental treatment, vaccine, or deadly medical procedure. Man-made toxic graphene does not belong in the human body. After reading these studies, I believe you will agree with the author that all Graphene Oxide use must end immediately and parties guilty of these heinous crimes against humanity must be brought to justice.
Graphene and Iron Oxide in Vaccines
From: ACS Publications, February 17, 2021, In Situ Transforming RNA Nanovaccines from Polyethylenimine Functionalized Graphene Oxide Hydrogel for Durable Cancer Immunotherapy,Yue Yin, Xiaoyang Li, Haixia Ma, Jie Zhang, Di Yu, Ruifang Zhao, Shengji Yu, Guangjun Nie, and Hai Wang
Abstract: Messenger RNA (mRNA) vaccine is a promising candidate in cancer immunotherapy as it can encode tumor-associated antigens with an excellent safety profile. Unfortunately, the inherent instability of RNA and translational efficiency are major limitations of RNA vaccine. Here, we report an injectable hydrogel formed with graphene oxide (GO) and polyethylenimine, which can generate mRNA and adjuvants (R848)-laden nanovaccines for at least 30 days after subcutaneous injection. The released nanovaccines can protect the mRNA from degradation and confer targeted delivering capacity to lymph nodes. The data show that this transformable hydrogel can significantly increase the number of antigen-specific CD8+ T cells and subsequently inhibit the tumor growth with only one treatment. Meanwhile, this hydrogel can generate an antigen specific antibody in the serum which in turn prevents the occurrence of metastasis. Collectively, these results demonstrate the potential of the PEI-functionalized GO transformable hydrogel for effective cancer immunotherapy.
The Food and Drug Administration (FDA) has approved many types of iron oxide nanoparticles for clinical use, such as treating iron deficiency, contrast agents for magnetic resonance imaging (MRI) and drug delivery platforms. In one study, researchers explored the combined use of iron oxide nanoparticles (superparamagnetic Fe3O4 nanoparticles) as a vaccine delivery platform and immune potentiator, and investigated how this formulation affected cytokine expression in macrophages and dendritic cells (DCs) in vitro and tumor growth in vivo. Their iron oxide nanoparticles greatly promoted the activation of immune cells and cytokine production, inducing potent humoral and cellular immune responses. These results suggest that this nanoparticle-based delivery system has strong potential to be utilized as a vaccine for viruses.
Superparamagnetic iron oxide nanoparticles (SPIONs) as a contrast agent have been widely used in magnetic resonance imaging for tumor diagnosis and theranostics. However, there has been safety concern of SPIONs with cirrhosis related to excess iron-induced oxidative stress. Analysis with PCR array of the toxicity pathways revealed the high dose of SPIONs induced significant expression changes of a distinct subset of genes in the cirrhosis liver. All these results suggested that excess iron of the high dose of SPIONs might be a risk factor for cirrhosis because of the marked impacts of elevated lipid metabolism, disruption of iron homeostasis and possibly, aggravated loss of liver functions.
At present, nanoparticles are used for various biomedical applications where they facilitate laboratory diagnostics and therapeutics. More specifically for drug delivery purposes, the use of nanoparticles is attracting increasing attention due to their unique capabilities and their negligible side effects not only in cancer therapy but also in the treatment of other ailments. Among all types of nanoparticles, biocompatible superparamagnetic iron oxide nanoparticles (SPIONs) with proper surface architecture and conjugated targeting ligands/proteins have attracted a great deal of attention for drug delivery applications.
Superparamagnetic iron oxide nanoparticles (SPIONs) have drawn attention because of their excellent superparamagnetic properties such as controllable size, large surface area-to-volume ratio, and nontoxicity. Surface functionalization of SPIONs with therapeutic molecules, including antimicrobial agents, has been successfully used in nanomedicine. Through application of an external magnetic field, antimicrobial-loaded SPIONs can be guided to the desired infection site allowing a direct and specific therapeutic effect with minimum side effects. The great advantage of SPIONs is their magnetic properties that allow direct delivery of matter into the pathogen zone without influencing the whole organism, which incites an increasing interest in the development of antimicrobial SPIONs.
When infused intravenously, these SPIONs can be used to detect and characterize small focal lesions in the liver. They also can be administered orally in order to visualize the digestive tract, and can be used as biomarkers to evaluate the efficacy of treatments. But still further investigations are required using labeled SPIONs in the field of molecular imaging.
Superparamagnetic iron oxide nanoparticles (SPIONs) have been studied for various biomedical applications, such as contrast agents, iron replacement therapies, drug delivery, tissue repair, hyperthermia, cell and tissue targeting, and transfection. SPIONs have an iron oxide core that is coated by an organic or inorganic layer. Bare SPIONs may be toxic because there is chemical reactive, so the coating layer prevents aggregation and agglomeration of the nanoparticles and reduces iron oxide oxidation. SPIONs are largely studied for magnetic resonance imaging and targeted delivery of drug and antigen to the required sites.
SPIONs have been approved by the FDA for treatment of anemia in adult patients with chronic renal disease. SPIONs are also used for noninvasive diagnosis of chronic liver diseases, nonalcoholic steatohepatitis, cirrhosis, liver tumors, magnetic resonance angiography, lymph node imaging, bone marrow imaging, and atherosclerotic plaque imaging.
Iron oxide Nanoparticles in Food
From: Science of Food, November 20, 2017, Is nano safe in foods? Establishing the factors impacting the gastrointestinal fate and toxicity of organic and inorganic food-grade nanoparticles, David Julian McClements & Hang Xiao
Nanotechnology offers the food industry a number of new approaches for improving the quality, shelf life, safety, and healthiness of foods. Nevertheless, there is concern from consumers, regulatory agencies, and the food industry about potential adverse effects (toxicity) associated with the application of nanotechnology in foods. In particular, there is concern about the direct incorporation of engineered nanoparticles into foods, such as those used as delivery systems for colors, flavors, preservatives, nutrients, and nutraceuticals, or those used to modify the optical, rheological, or flow properties of foods or food packaging. This review article summarizes the application of both inorganic (silver, iron oxide, titanium dioxide, silicon dioxide, and zinc oxide) and organic (lipid, protein, and carbohydrate) nanoparticles in foods, highlights the most important nanoparticle characteristics that influence their behavior, discusses the importance of food matrix and gastrointestinal tract effects on nanoparticle properties, emphasizes potential toxicity mechanisms of different food-grade nanoparticles, and stresses important areas where research is still needed. The authors note that nanoparticles are already present in many natural and processed foods, and that new kinds of nanoparticles may be utilized as functional ingredients by the food industry in the future.
Nanotechnology can be utilized to improve food quality, shelf life, safety, cost, and nutritional benefits. In some cases, the nanomaterials used in the food industry are not intended to find their way into the final food product, e.g., those used in packaging, sensors, and antimicrobial treatments designed for sanitizing food manufacturing plants. Engineered nanoscale materials (ENMs) may be intentionally added to foods or they may inadvertently find their way into foods (such as nanoparticles in packaging materials that leach into the food matrix). ENMs may be used to create delivery systems for nutrients, nutraceuticals, colors, flavors, and preservatives, or they may be used to modify the texture, appearance, or stability of foods. Nanoscale structures may be present in foods as the result of routinely used food processing operations, such as homogenization, grinding, and cooking.
Nanoparticles present in foods can be categorized as either organic or inorganic. Inorganic materials, such as silver, iron oxide, titanium dioxide, silicon dioxide, or zinc oxide are commonly used. These particles are either crystalline or amorphous solids at ambient temperature, which may be spherical or non-spherical, have different surface characteristics and coatings, and come in different sizes depending on the initial materials and preparation conditions used in their fabrication.
Silver nanoparticles are used as antimicrobial agents in foods and food packaging materials.
Zinc oxide nanoparticles may be used as a source of zinc and in food packaging as antimicrobial agents to prevent contamination of foods and as ultraviolet light absorbers.
Iron oxide nanoparticles are utilized in foods as colorants or sources of bioavailable iron and come in different sizes, shapes, and crystalline forms.
Titanium dioxide nanoparticles are used as functional ingredients in certain foods to provide characteristic optical properties such as increased lightness and brightness.
Silicon dioxide nanoparticles are added to certain powdered foods as anticaking agents to enhance flow properties, e.g., salts, icing sugar, spices, dried milk, and dry mixes.
Lipid nanoparticles are widely present within many commercial food products, like beverage emulsions, such as soft drinks, fortified waters, fruit juices, and dairy drinks, contain small oil droplets dispersed in water.
Protein nanoparticles are the casein micelles found in bovine milk and other dairy products, which are small clusters of casein molecules and calcium phosphate ions.
Carbohydrate nanoparticles are typically assembled from digestible or indigestible polysaccharides, such as starch, cellulose, alginate, carrageenan, pectin, and xanthan and they may be indigestible within the upper gastrointestinal tract (GIT).
Some organic substances used to fabricate food nanoparticles (such as dietary fibers and mineral oils) may not be digested in the upper GIT. Inorganic nanoparticles are also not digested in the GIT. Any nanoparticles that are not digested or absorbed in the upper GIT will reach the lower GIT where they may alter the microbiome in a negative way. The ability of inorganic nanoparticles to produce toxicity is often associated with their chemical reactivity, which depends on their composition. For example, some inorganic nanoparticles dissolve and release ions that promote undesirable chemical or biochemical reactions (e.g., silver nanoparticles).
Ingested nanoparticles accumulate in numerous tissues. These nanoparticles travel across the mucus layer and are then absorbed by active or passive transport mechanisms. After they have been absorbed into the cells, they accumulate within the cells. The accumulation of nanoparticles within specific tissues may lead to long-term problems if they exhibit toxic effects above a certain accumulation threshold. This mechanism of action is likely to be most important for inorganic nanoparticles that are bio-persistent (not normally digested or metabolized in GIT).
Nanoparticles may produce toxicity in cells through a variety of different mechanisms. One of the most important factors contributing to the toxicity of inorganic nanoparticles is their ability to generate reactive oxygen species (ROS), such as singlet oxygen, superoxide, hydrogen peroxide and hydroxyl radicals. These ROS may then cause damage to cell membranes, organelles, and the nucleus by interacting with lipids, proteins, or nucleic acids. As a result, many biochemical functions required to maintain cell viability, such as ATP production, DNA replication, and gene expression, may be adversely affected. A number of studies have reported the ability of inorganic nanoparticles to increase the generation of ROS in cells and to produce cytotoxicity.
The ability of nanoparticles to greatly increase the oral bioavailability of hydrophobic substances does have adverse health effects by promoting the uptake of undesirable non-polar substances in foods, such as certain pesticides (glyphosates, etc.) and hormones. For example, a food product that contains lipid nanoparticles (such as a beverage, sauce, dressing, or cream) may increase the bioavailability of hydrophobic pesticides on fruits or vegetables consumed with them.
Graphene Self-Assembles into Blood Vascular Structures
From: Materials Today Connecting the Materials Community, March 19, 2020, New graphene-based material self-assembles into vascular structures
An international team of scientists, led by Alvaro Mata at the University of Nottingham and Queen Mary University London in the UK, has discovered a new material that can be 3D printed to create tissue-like vascular structures. In a paper in Nature Communications, the scientists report developing a way to 3D print graphene oxide with a protein that can organize into tubular structures that replicate some of the properties of vascular tissue.
“This work offers opportunities in bio-fabrication by enabling simultaneous top-down 3D bioprinting and bottom-up self-assembly of synthetic and biological components in an orderly manner from the nanoscale,” said Mata. “Here, we are bio-fabricating micro-scale capillary-like fluidic structures that are compatible with cells, exhibit physiologically relevant properties, and have the capacity to withstand flow. This could enable the recreation of vasculature in the lab and have implications in the development of safer and more efficient drugs, meaning treatments could potentially reach patients much more quickly.”
Self-assembly is the process by which multiple components spontaneously organize into larger, well-defined structures. Biological systems rely on this process to controllably assemble molecular building blocks into complex and functional materials exhibiting remarkable properties such as the capacity to grow, replicate and perform robust functions. The new biomaterial is produced by the self-assembly of a protein with graphene oxide. This self-assembly process allows the flexible regions of the protein to order and conform to the graphene oxide, generating a strong interaction between them. By controlling the way in which the two components are mixed, it is possible to guide their assembly at multiple scales in the presence of cells to produce complex robust structures.
Self-Assembling Graphene Nanotubes
From: Angewandte Chemie, First published: March 14, 2001, Self-Assembling Organic Nanotubes, T. Bong,Thomas D. Clark Dr., Juan R. Granja Prof. Dr., M. Reza Ghadiri Prof.
Hollow tubular structures of molecular dimensions perform diverse biological functions in nature. Examples include scaffolding and packaging roles played by cytoskeletal microtubules and viral coat proteins, respectively, as well as the chemical transport and screening activities of membrane channels. In the preparation of such tubular assemblies, biological systems make extensive use of self-assembling and self-organizing strategies. Owing to numerous potential applications in areas such as chemistry, biology, and materials science considerable effort has recently been devoted to preparation of artificial nanotubular structures. This article reviews design principles and the preparation of synthetic organic nanotubes, with special emphasis on noncovalent processes such as self-assembly and self-organization.
Programmable Living Systems
From: Nature Reviews Materials, Materials design by synthetic biology, Tzu-Chieh Tang, Bolin An, Yuanyuan Huang, Sangita Vasikaran, Xiaoyu Jiang
Synthetic biology applies genetic tools to engineer living cells and organisms analogous to the programming of machines. In materials synthetic biology, engineering principles from synthetic biology and materials science are integrated to redesign living systems as dynamic and responsive materials with emerging and programmable functionalities. In this Review, we discuss synthetic-biology tools, including genetic circuits, model organisms and design parameters, which can be applied for the construction of smart living materials. We investigate non-living and living self-organizing multifunctional materials, such as intracellular structures and engineered biofilms, and examine the design and applications of hybrid living materials, including living sensors, therapeutics and electronics, as well as energy-conversion materials and living building materials. Finally, we consider prospects and challenges of programmable living materials and identify potential future applications.
Engineered Living Materials
From: MIT Libraries, Towards engineering living functional materials, 2021, Tang, Tzu-Chieh,Ph. D.Massachusetts Institute of Technology
The field of engineered living materials (ELMs) aims to recapitulate the remarkable properties of natural biology to create novel, growable, multifunctional materials using genetically engineered organisms. Most relevant pioneering work was created using nano- to microscale biofilm [GO], which has rather small yields and usually requires costly modification. Second, releasing genetically modified microorganisms (GMMs) into the field for food, water, or agricultural applications is often considered risky due to the uncertainty of wild-type organisms acquiring undesirable traits, such as antibiotic resistance, from the GMMs. A significant effort in addressing these unmet needs is called for. This Thesis starts with an introduction of genetic circuits and an in-depth review of the current trends in materials synthetic biology, which includes two major categories of ELMs: self-organizing functional materials and hybrid living materials. The following chapters describe the technologies developed to achieve high scalability and safe deployment of ELMs in these two categories and living devices suitable for real-world applications.
Graphene Oxide Toxicity
From: Biomedical Research International, Volume 2021 |Article ID 5518999, Synthesis and Toxicity of Graphene Oxide Nanoparticles: A Literature Review of In Vitro and In Vivo Studies, Asmaa Rhazouani, Halima Gamrani , Mounir El Achaby , Khalid Aziz, Lhoucine Gebrati, Md Sahab Uddin, and Faissal AZIZ, https://doi.org/10.1155/2021/5518999
Nanomaterials have been widely used in many fields in the last decades, including electronics, biomedicine, cosmetics, food processing, buildings, and aeronautics. The application of these nanomaterials in the medical field could improve diagnosis, treatment, and prevention techniques. Graphene oxide (GO), an oxidized derivative of graphene, is currently used in biotechnology and medicine for cancer treatment, drug delivery, and cellular imaging. Also, GO is characterized by various physicochemical properties, including nanoscale size, high surface area, and electrical charge. However, the toxic effect of GO on living cells and organs is a limiting factor that limits its use in the medical field. Recently, numerous studies have evaluated the biocompatibility and toxicity of GO in vivo and in vitro. In general, the severity of this nanomaterial’s toxic effects varies according to the administration route, the dose to be administered, the method of GO synthesis, and its physicochemical properties.
Nanoparticles are widely used in electronics, aeronautics, energy, agriculture, cosmetics, medicine, textile production, and many other fields. They are currently used to administer drugs, proteins, genes, vaccines, polypeptides, and nucleic acids. GO is a nanomaterial that has been known for more than 150 years and is used in many applications. In recent years, graphene has been exploited in the medical field, particularly for DNA sequencing, the development of biosensors, and cell differentiation and growth. As graphene is insoluble in water, its applications are limited to passive platforms for detection and cell work. Its functional derivative GO has unique properties that make it more effective for biomedical applications. It is characterized by its ability to disperse in many solvents, facilitating its handling. In addition, GO is used to administer anticancer drugs in biological cells, aptamers for ATP probing in epithelial cells, and gene delivery. These nanomaterials have a large surface area and can maintain drugs’ stability without altering the biological activity, much more than other nanomaterials.
GO is characterized by properties that make it attractive in other areas such as sensors and energy storage. As applications increase, exposure to GO increases across populations. These include exposures during nanomaterial manufacturing and biomedical treatment. GO is involved in many applications, but there is one main factor limiting “its toxicity” limiting its use. Researchers are often faced with the problem of balancing the positive therapeutic effects of GO with the side effects associated with its toxicity
Graphene Oxide as a Vaccine Carrier and Adjuvant
From: Acta Biomaterialia, Volume 112, August 2020, Pages 14-28, Recent progress of graphene oxide as a potential vaccine carrier and adjuvant, WanjunCaoab, LinHea, Weidong Caob, Xiaobing HuangaKun, Jiac Jingying Dai
Adjuvants and carriers have been appropriately added to the vaccine formulation to improve the immunogenicity of the antigen and induce long-lasting immunity. Graphene oxide (GO), widely employed for the delivery of biomolecules, excels in loading and delivering antigen and shows the potentiality of activating the immune system. However, GO aggregates in biological liquid [blood clots] and induces cell death, and it also exhibits poor bio-solubility and bio-compatibility. To address these limitations, various surface modification protocols have been employed to integrate aqueous compatible substances with GO to effectively improve its biocompatibility. More importantly, these modifications render functionalized-GO with superior properties as both carriers and adjuvants. Due to its unique physicochemical properties, graphene oxide is widely employed in medicine for purposes of photothermal treatment of cancer, drug delivery, antibacterial therapy, and medical imaging. Our work describes the surface modification of graphene oxide and for the first time summarizes that functionalized graphene oxide serves as a vaccine carrier and shows significant adjuvant activity in activating cellular and humoral immunity.
Precision medicine informs us that graphene oxide has been studied for its promising uses in a wide variety of nanomedical applications including tissue engineering, cancer treatment, medical imaging, and drug delivery. Its physiochemical properties allow for a structure to regulate the behavior of stem cells, with the potential to assist in the intracellular delivery of DNA, growth factors, and synthetic proteins that could allow for the repair and regeneration of muscle tissue. Due to its unique behavior in biological environments, graphene oxide has also been proposed as a novel material in early cancer diagnosis. It has also been explored for its uses in vaccines and immunotherapy, including as a dual-use adjuvant and carrier of biomedical materials.
Several typical mechanisms underlying graphene oxide nanomaterial’s toxicity have been revealed, for instance, physical destruction, oxidative stress, DNA damage, inflammatory response, apoptosis, autophagy, and necrosis. In these mechanisms, toll-like receptors (TLR), transforming growth factor-beta (TGF-β) and tumor necrosis factor-alpha (TNF-α) dependent-pathways are involved in the signaling pathway network, and oxidative stress plays a crucial role in these pathways. Many experiments have shown that graphene oxide nanomaterials have toxic side effects in many biological applications. According to the USA FDA, graphene, graphene oxide, and reduced graphene oxide elicit toxic effects both in vitro and in vivo. Graphene-family nanomaterials (GFN) are not approved by the USA FDA for human consumption.
Graphene Oxide-incorporated Hydrogels in Medicine
From: Polymer Journal, Volume 52, pages 823-837, May 8, 2020, Graphene oxide-incorporated hydrogels for biomedical applications, Jongdarm Yi, Goeun Choe, Junggeon Park Young Lee
Graphene and graphene derivatives (e.g., graphene oxide) have been incorporated into hydrogels to improve the properties (e.g., mechanical strength) of conventional hydrogels and/or develop new functions (e.g., electrical conductivity and drug loading/delivery). Unique molecular interactions between graphene derivatives and various small or macromolecules enable the fabrication of various functional hydrogels appropriate for different biomedical applications. In this mini-review, we highlight the recent progress in GO-incorporated hydrogels for biomedical applications while focusing on their specific uses as mechanically strong materials, electrically conductive scaffolds/electrodes, and high-performance drug delivery vehicles.
Graphene Oxide in Vaccines
From: Nanoscale, Functionalized graphene oxide serves as a novel vaccine nano-adjuvant for robust stimulation of cellular immunity, Ligeng Xu, Jian Xiang, Ye Liu, Jun Xu, Yinchan Luo, Liangzhu Feng, Zhuang Liu and Rui Peng
Benefiting from their unique physicochemical properties, graphene derivatives have attracted great attention in biomedicine. In this study, we carefully engineered graphene oxide (GO) as a vaccine adjuvant for immunotherapy using urease B (Ure B) as the model antigen. Our work not only presents a novel, highly effective GO-based vaccine nano-adjuvant, but also highlights the critical roles of surface chemistry for the rational design of nano-adjuvants.
What if it were announced that CANDACE OWENS had married Alexander Soros, son of George Soros. Conservatives would be outraged, yet Candace married George Farmer, son of Baron Michael Farmer and … crickets.
Candace married George Farmer, son of the equally notorious bad boy Baron Michael Farmer, yet places like Turning Point USA-UK and WND (which supports her recent BLEXIT campaign) support her like she’s America’s special patriot darling.
Who is Michael Farmer?
Michael Farmer, ranked with Soros, Icahn, Slim, Bogle
We will posting the answer to this quiz in our next report. Hint: It concerns Candace Owen’s father-in-law and a company that tried to take over America before it went bankrupt.
Next time Candace is receiving questions from her audience or you have an opportunity to ask her an online questions, inquire about her husband’s relationship to the Pilgrims Society, George Soros, and silver/gold rigging. If she doesn’t know, then it is true – her head is as empty as her American patriotism .
During War, everything that was previously illegal, becomes illegal, acceptable and kept very top secret. Nothing is recorded. No one ever finds out about it. Americans have never seen War on their soil, however, america has brought war to a great part of the world, that did not want wars. Eventually the tables turn. I am very sad about what is coming, but the world wants to bring america to its knees. You have no idea how hated america is right now. During Wars, there are no freedoms or human rights. There is only this: “The living will envy the dead”. War is Hell. WE must all ask for Mercy and forgiveness in our prayers and pray for PEACE in america every day. There is no good side in any war. Quite the contrary. War is a satanic ritual.